# FDA recall Z-2407-2020

> **Utak Laboratories Inc** · Class III · device recall initiated 2020-03-20.

## Product

Utak NR Trace Elements Serum Control, 5 ml, REF 66816.  The responsible firm on the label is UTAK LABORATORIES, INC., Valencia, CA. Control for in vitro diagnostics.

## Reason for recall

The product has an incorrect reference value for cadmium and an incorrect expected range.

## Distribution

Worldwide Distribution. US nationwide, Canada, Australia, France, Germany, Israel, Italy, New Zealand, Philippines, and United Kingdom.

## Key facts

- **Recall number:** Z-2407-2020
- **Recalling firm:** Utak Laboratories Inc
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-20
- **Report date:** 2020-07-01
- **Termination date:** 2020-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Valencia, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2407-2020

## Citation

> AI Analytics. FDA recall Z-2407-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2407-2020. Source: US FDA. Licensed CC0.

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